search
Back to results

Anastomotic Leakage Following Laparoscopic Resection for Rectal Cancer

Primary Purpose

Anastomotic Leakage

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Laparoscopic resection for rectal cancer
Sponsored by
Mansoura University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Anastomotic Leakage focused on measuring Anastomotic leakage, Rectal cancer, Laparoscopic, Rectal resection

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients who undergo laparoscopic resection for biopsy proven rectal cancer.

Exclusion Criteria:

  • Open surgery,
  • Emergency intervention,
  • Palliative resection,
  • Stage IV with distant metastasis,
  • Recurrent cancer,
  • Multivisceral resection

Sites / Locations

  • Mansoura University Hospitals
  • Policlinico Tor Vergata Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Rectal cancer patients

Arm Description

All patients who will fulfill the inclusions criteria. Patients will undergo formal curative radical Laparoscopic resection for rectal cancer

Outcomes

Primary Outcome Measures

Incidence of anastomotic leakage
Incidence of anastomotic leakage in patients who underwent laparoscopic resection of rectal cancer. This including clinical and sub-clinical (radiological diagnosis) leakage.

Secondary Outcome Measures

Role of diversion in prevention of anastomotic leakage.
Do the patients with diversion have low incidences of anastomotic leakage compared to those without.
Management of anastomotic leakage
The comparison of conservative, radio-logical, or surgical options.
Oncological outcomes of anastomotic leakage
For patients who complete 24 months of follow-up for local recurrence.
30 days postoperative morbidity and mortality
In the first 30 days postoperative

Full Information

First Posted
March 12, 2016
Last Updated
May 27, 2020
Sponsor
Mansoura University
Collaborators
University of Rome Tor Vergata
search

1. Study Identification

Unique Protocol Identification Number
NCT02718729
Brief Title
Anastomotic Leakage Following Laparoscopic Resection for Rectal Cancer
Official Title
Anastomotic Leakage Following Laparoscopic Resection for Rectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
June 1, 2015 (Actual)
Primary Completion Date
January 1, 2017 (Actual)
Study Completion Date
June 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mansoura University
Collaborators
University of Rome Tor Vergata

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anastomotic leak (AL) is a breakdown of a suture line in a surgical anastomosis with a subsequent leakage of the luminal content. Anastomotic leakage occurs commonly in rectal and esophageal anastomosis than the other parts of the alimentary tract due to technical difficulties in accessing these areas and their easily compromised blood supply. Anastomotic leakage is the most feared complication following rectal resection and anastomosis. The incidence of anastomotic leakage ranges from 2.8% to more than 15%, with mortality rate more than 30%. Subclinical anastomotic failure may occur in up to 51% of patients. Anastomotic leakage leads to increase the rate of secondary interventions, re-operations, longer postoperative hospital stay, increased cost, and major impact on the patient's quality of life. In the medium to long term, patient may be unfit for post-operative adjuvant therapy with decreased the disease survival. Furthermore anastomotic leakage itself may increase the local recurrence, a reduction in overall survival, and a large proportion of patients are left with a permanent stoma.
Detailed Description
Study populations: all patients will sign an informed consent prior to the surgery to be included in the study, after explanation of the nature of the disease, possible treatment, and the possibility of stoma formation. Data recording: basic demographic data are recorded including age and sex of the patient as well as detailed information on history, risk factors, preoperative diagnostics, surgical procedure, intraoperative findings, histopathological work-up, and postoperative course. Variables analysis: the variables are divided into patient-related, tumor-related, therapy-related, and techniques-related variables. Preoperative workup: all patients will have detailed clinical history and physical examination including DRE. Routine laboratory investigations also are included e.g. CBC, blood glucose level, liver, and kidney function tests. Regular workup for rectal cancer are included; full colonoscopy with biopsy, gastrografin/barium enema, TRUS evaluate degree of invasion of the rectal wall and regional lymph nodes, abdominal and pelvic CT scan, Chest x-ray or CT scan, CEA level, and EORTC Quality of life Questionnaire. Level of the tumor: is measured from the lower border of the tumor to the anal verge by the rigid sigmoidoscope; considering it low < 6 cm, middle 6-12 cm, and upper > 12 cm. Preoperative preparation: all patients will have preoperative mechanical bowel preparation and adequate thromboembolic prophylaxis. Prophylactic antibiotics will be given 30 - 60 minutes before surgery. A surgeon or stoma therapist will mark the site of the stoma before the operation in all patients. Level of the anastomosis: is measured from the anastomosis to the anal verge by the rigid sigmoidoscope intraoperative; considering it low < 10 cm, middle 10-15 cm, and upper > 15 cm. The rectal anastomosis is tested intraoperative with: trans-anal air insufflation with the pelvis immersed with saline to detect bubbles, trans-anal introduction of dye, or competence of donuts in stapled anastomosis. Postoperative follow up: Access the postoperative condition locally and systemically by bedsides clinical parameters, and usual blood tests like leucocyte count and CRP level at the 3rd and the 7th day postoperative. Radiological follow up by Gastrografin enema around the 10th day or before dismissal from the hospital. Abdominal and pelvic CT scan is ordered in patients with clinical deterioration, abnormal abdominal findings, and turbid drainage secretion. Peritoneal samples are collected from the abdominal drains at the first, third, and fifth days postoperatively for peritoneal microbiological study and cytokines (IL-6, IL-10, and TNF) level measurement. Patients will receive a Quality of Life questionnaire (EORTC 30, 38) preoperatively, 30 days postoperative, and 30 days after stoma closure in case of diversion. Follow up of patients continue till discharge, and 30 days postoperative. In cases with diversion follow up will continue till closure of stoma and 30 days after closure. Stoma closure in an uneventful course will be scheduled 8-10 weeks after the primary operation. Diagnosis of leakage: Fecal secretion via indwelling abdominal drainage, surgical wound or vagina. Radiological via fluid collection adjacent to anastomosis associated with extraluminal contrast extravasation. Classification of leakage: patients classified according to leakage into: Non leakage group. Leakage group, radiological is asymptomatic and detected on imaging, localized is diagnosed on radiological findings of a pelvic collection and clinically do not require a laparotomy or laparoscopy, and generalized is confirmed at laparotomy or laparoscopy. Outcomes: Primary outcomes: Incidences of anastomotic leakage following laparoscopic resection for rectal cancer. 30 day's postoperative morbidity and mortality. secondary outcomes: The role of diversion on prevention of anastomotic leakage, are patients with diversion have low incidences of leakage. Management of anastomotic leakage. Effect of anastomotic leakage on oncological outcome, assessment of local recurrence after 24 months follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anastomotic Leakage
Keywords
Anastomotic leakage, Rectal cancer, Laparoscopic, Rectal resection

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
59 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rectal cancer patients
Arm Type
Other
Arm Description
All patients who will fulfill the inclusions criteria. Patients will undergo formal curative radical Laparoscopic resection for rectal cancer
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic resection for rectal cancer
Intervention Description
Formal curative radical laparoscopic rectal resection.
Primary Outcome Measure Information:
Title
Incidence of anastomotic leakage
Description
Incidence of anastomotic leakage in patients who underwent laparoscopic resection of rectal cancer. This including clinical and sub-clinical (radiological diagnosis) leakage.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Role of diversion in prevention of anastomotic leakage.
Description
Do the patients with diversion have low incidences of anastomotic leakage compared to those without.
Time Frame
2 years
Title
Management of anastomotic leakage
Description
The comparison of conservative, radio-logical, or surgical options.
Time Frame
2 years
Title
Oncological outcomes of anastomotic leakage
Description
For patients who complete 24 months of follow-up for local recurrence.
Time Frame
2 years
Title
30 days postoperative morbidity and mortality
Description
In the first 30 days postoperative
Time Frame
30 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients who undergo laparoscopic resection for biopsy proven rectal cancer. Exclusion Criteria: Open surgery, Emergency intervention, Palliative resection, Stage IV with distant metastasis, Recurrent cancer, Multivisceral resection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mostafa Shalaby, M,D., MSc.
Organizational Affiliation
Mansoura University/ University of Rome Tor Vergata
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mansoura University Hospitals
City
Mansoura
State/Province
Al Dakhlia
ZIP/Postal Code
35516
Country
Egypt
Facility Name
Policlinico Tor Vergata Hospital
City
Rome
ZIP/Postal Code
00133
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Anastomotic Leakage Following Laparoscopic Resection for Rectal Cancer

We'll reach out to this number within 24 hrs